CAS 17042-40-9
:4-METHOXYPHENYL 2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSIDE
Description:
4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranoside is a glycoside compound characterized by its structural components, which include a methoxyphenyl group and a D-mannopyranoside moiety that is fully acetylated at the hydroxyl positions. This compound is typically used in organic synthesis and carbohydrate chemistry due to its ability to participate in glycosylation reactions. The presence of the acetyl groups enhances the stability and solubility of the molecule, making it more amenable to various chemical transformations. Its methoxyphenyl substituent can also influence its reactivity and interaction with other molecules. The compound is generally white to off-white in appearance and may exhibit specific optical activity due to its chiral centers. As with many glycosides, it may have applications in the development of pharmaceuticals or as intermediates in the synthesis of more complex carbohydrates. Proper handling and storage conditions are essential to maintain its integrity and prevent degradation.
Formula:C21H26O11
InChI:InChI=1/C21H26O11/c1-11(22)27-10-17-18(28-12(2)23)19(29-13(3)24)20(30-14(4)25)21(32-17)31-16-8-6-15(26-5)7-9-16/h6-9,17-21H,10H2,1-5H3/t17-,18-,19+,20+,21+/m1/s1
InChI key:InChIKey=RPHXBVOPPUTUES-MJCUULBUSA-N
SMILES:O(C(C)=O)[C@@H]1[C@H](OC(C)=O)[C@@H](OC2=CC=C(OC)C=C2)O[C@H](COC(C)=O)[C@H]1OC(C)=O
Synonyms:- 4-Methoxyphenyl2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside
- Mannopyranoside, p-methoxyphenyl, tetraacetate, α-<span class="text-smallcaps">D</span>-
- α-<span class="text-smallcaps">D</span>-Mannopyranoside, 4-methoxyphenyl, 2,3,4,6-tetraacetate
- α-<span class="text-smallcaps">D</span>-Mannopyranoside, 4-methoxyphenyl, tetraacetate
- Mannopyranoside, p-methoxyphenyl, tetraacetate, α-D-
- α-D-Mannopyranoside, 4-methoxyphenyl, tetraacetate
- 4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
- α-D-Mannopyranoside, 4-methoxyphenyl, 2,3,4,6-tetraacetate
- (2R,3R,4S,5S,6R)-2-(Acetoxymethyl)-6-(4-methoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
- O
- 4-METHOXYPHENYL 2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSIDE
- -acetyl-&alpha
- 4-Methoxyphenyl2,3,4,6-Tetra-O-acetyl-α-D-mannopyranoside>
- 4-Methoxyphenyl alpha-D-mannopyranoside tetraacetate
- 4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside ,98%
- 4-METHOXYPHENYL 2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSIDE USP/EP/BP
- 4-Methoxyphenyl-2,3,4,6-tetra-O-acetyl-β-D-mannopyranoside
- p-methoxyphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
- (2R,3R,4S,5S,6R)-3,4,5-tris(acetyloxy)-6-(4-methoxyphenoxy)oxan-2-yl]methyl acetate
- 4-Methoxyphenyl 2,3,4,6-Tetra-
- See more synonyms
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4-Methoxyphenyl 2,3,4,6-Tetra-O-acetyl-alpha-D-mannopyranoside
CAS:Formula:C21H26O11Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:454.434-Methoxyphenyl 2,3,4,6-Tetra-O-acetyl-α-D-mannopyranoside
CAS:4-Methoxyphenyl 2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosideFormula:C21H26O11Purity:>98%Molecular weight:454.434-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
CAS:4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is a biochemical reagent utilized in glycobiology research, which examines the structure, synthesis, biology, and evolution of carbohydrates. This field encompasses carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. Glycobiology closely relates to fundamental research, biomedicine, and biotechnology.Formula:C21H26O11Molecular weight:454.42454-Methoxyphenyl 2,3,4,6-Tetra-O-acetyl-α-D-mannopyranoside
CAS:Formula:C21H26O11Purity:98%Molecular weight:454.4245





